US3644150A - Stabilizing of aqueous solutions of potassium persulphate - Google Patents

Stabilizing of aqueous solutions of potassium persulphate Download PDF

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Publication number
US3644150A
US3644150A US874962A US87496269A US3644150A US 3644150 A US3644150 A US 3644150A US 874962 A US874962 A US 874962A US 87496269 A US87496269 A US 87496269A US 3644150 A US3644150 A US 3644150A
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United States
Prior art keywords
acid
potassium
potassium persulphate
aqueous solution
stabilizer
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Expired - Lifetime
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US874962A
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English (en)
Inventor
Joris Jan Cornelis Oomen
Jan Adrianus Visser
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US Philips Corp
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US Philips Corp
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/04Cells with aqueous electrolyte
    • H01M6/045Cells with aqueous electrolyte characterised by aqueous electrolyte
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/055Peroxyhydrates; Peroxyacids or salts thereof
    • C01B15/06Peroxyhydrates; Peroxyacids or salts thereof containing sulfur
    • C01B15/08Peroxysulfates
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/16Acidic compositions
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/04Cells with aqueous electrolyte

Definitions

  • the invention relates to stabilized aqueous solutions of potassium persulfate, and particularly to a primary cell in which potassium persulfate is used as a depolarizer.
  • potassium persulfate in an aqueous solution is unstable. Such potassium persulfate solutions decompose while releasing oxygen. Attempts have been made to increase the stability of potassium persulfate in aqueous solutions by addition of other potassium salts which are satisfactorily soluble in water such as potassium chloride. Stabilizer effects however of these salts are only minor.
  • the invention relates to an aqueous solution of potassium persulfate, and is characterized in that this solution contains a potassium of an organic sulfonic acid whose solubility in water of 25 C. is larger than 1 g. eq./l.
  • a salt both in a solid state and in a solution, is referred to in this respect as a stabilizer.
  • Suitable stabilizers are especially potassium salts of methane mono sulfonic acid, ethane disulfonic acid, ethane trisulfonic acid, benzene disulfonic acid, benzene trisulfonic acid.
  • Aqueous solutions of potassium persulfate are, inter alia, used as oxidants for pigmentation agents, as etchants for metals and as depolarizers in primary cells.
  • the invention may advantageously be used. This particularly applies to the use for primary cells in which potassium persulfate is used as a depolarizer.
  • the invention therefore particularly relates to a primary cell in which potassium persulphate as a depolarizer and a stabilizer have been used according to the invention.
  • An embodiment of a primary cell according to the invention is the one in which the anode consists of zinc, the separator consists of a cation-exchanging diaphragm, and the cathode, also sometimes called depolarizer mass, consists of a compressed mass mainly comprising pulverulent carbon, for example, graphite or carbon felt, and includes a depolarizer and a stabilizer and wherein furthermore a collector, for example, a rod or plate of graphite is used.
  • Primary cells according to the invention may be manufactured in manners known for such cells.
  • the corrosion resistance of the zinc anode may be enhanced in known manner by treatment with a mercuric chloride solution.
  • Cation-exchanging diaphragms which are known per se and consist, for example, of a sulfonated copolymer of styrene and divinyl benzene, may be used as separators. Such diaphragms are also sometimes called negative diaphragms. They prevent the passage of negative ions, but allow the positive ions, the cations, to pass.
  • pulverulent graphite may be used, for example, for the carbon to be used in the depolarizer mass.
  • Carbon felt is preferred, inter alia, because this can more easily be purified by a pretreatment from substances which promote the decomposition of potassium persulphate; purification may be effected, for example, by etching with a mixture of chromium acid-sulfuric acid-water.
  • the starting material may be a mixture of pulverulent carbon or carbon felt and pulverulent potassium persulphate. This mixture may also contain a stabilizer in a pulverulent form.
  • the applicant has found by experiments that there is a relationship between the stabilizing action of a stabilizer and the solubility thereof in water. The greater this solubility the greater the stabilizing action.
  • the following stabilizers are therefore preferred: potassium salt of benzene disulphonic acid, of benzene trisulphonic acid. and of methane monosulphonic acid. in the given sequence.
  • the concentration of stabilizer is to be preferably at least 1.5 g. eq./l. for a satisfactory stabilizing action in the cathode liquid (which is the liquid contained in the cathode space with which liquid also the depolarizer mass is soaked). Furthermore it has been found that when increasing the concentration of stabilizer to more than 2.5 g. eq./1. stabilizing action substantially does not increase any more, or in other words, at a concentration of approximately 2.5 g. eq./l. the stabilizing action is optimum.
  • the stabilizing action of a stabilizer may be increased by incorporating in the depolarizer mass a substance acting as a buffer so that the pH in this mass is maintained between 5.5 and 8.5 and preferably between 6 and 8.
  • Suitable substances are particularly zinc oxide, aluminum oxide which has not been rendered entirely anhydrous and aluminum hydroxide.
  • the experiments were performed in a glass vessel provided with a calibrated tube, in which the evolved gas was collected.
  • the amount of evolved gas was determined from day to day.
  • the Table below shows in how many days 1 ml. ofgas had been evolved.
  • experimental mixture contained: for experiment A: 3.0 g. eq./l. potassium chloride. B: 1.5 g. eq./l. potusxium uulfutc. C: 0.5 g. eq./l. mcthune monopolutisium xulfonute. D: 1.0 g. q./1. melhune monopotussium sulfonulc. E: 1.5 g. eqJl. methane monopotussium sulfonale. F: 3.0 g. eq./l. methane monopotassium sulfunule. G: 0.5 g. eq./l.
  • H 1.0 g. eq./l. benzcnelJ'dipotassium sulfonale.
  • l 1.5 g. e ./l. benzene-l.3-dipotassium sulfonate.
  • K 3.0 g. eq./l. benzene-1,3-dipotassium sulfonate;
  • L 3.0 g. eq./l. benzene-l .S-S-tripotassium sulfonutc.
  • An aqueous solution of potassium persulphate characterized in that this solution contains as a stabilizer a potassium salt of an organic sulphonic acid whose solubility in water of 25 C. is larger than 1 g. eq-ll.
  • An aqueous solution of potassium persulphate as claimed in claim 1. characterized in that a potassium salt of methane monosulphonic acid. methane disulphonic acid. methane trisulphonic acid. ethane disulphonic acid. ethane trisulphonic nun-u in claim 4, characterized in that a substance acting as a buffer is used which maintains the pH of the solution between 5.5 and 8.5 and preferably between 6.0 and 8.0.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Electrochemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Metallurgy (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Hybrid Cells (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US874962A 1968-10-12 1969-11-07 Stabilizing of aqueous solutions of potassium persulphate Expired - Lifetime US3644150A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL6814635A NL6814635A (enrdf_load_html_response) 1968-10-12 1968-10-12

Publications (1)

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US3644150A true US3644150A (en) 1972-02-22

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US874962A Expired - Lifetime US3644150A (en) 1968-10-12 1969-11-07 Stabilizing of aqueous solutions of potassium persulphate

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US (1) US3644150A (enrdf_load_html_response)
JP (1) JPS4816094B1 (enrdf_load_html_response)
DE (1) DE1950030A1 (enrdf_load_html_response)
FR (1) FR2020578A1 (enrdf_load_html_response)
GB (1) GB1237309A (enrdf_load_html_response)
NL (1) NL6814635A (enrdf_load_html_response)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4312929A (en) * 1979-05-03 1982-01-26 Ebauches S.A. Polymeric electrolyte for electro-optical device
WO2011130622A1 (en) 2010-04-15 2011-10-20 Advanced Technology Materials, Inc. Method for recycling of obsolete printed circuit boards
US9221114B2 (en) 2011-12-15 2015-12-29 Advanced Technology Materials, Inc. Apparatus and method for stripping solder metals during the recycling of waste electrical and electronic equipment

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4312929A (en) * 1979-05-03 1982-01-26 Ebauches S.A. Polymeric electrolyte for electro-optical device
WO2011130622A1 (en) 2010-04-15 2011-10-20 Advanced Technology Materials, Inc. Method for recycling of obsolete printed circuit boards
US9215813B2 (en) 2010-04-15 2015-12-15 Advanced Technology Materials, Inc. Method for recycling of obsolete printed circuit boards
US10034387B2 (en) 2010-04-15 2018-07-24 Entegris, Inc. Method for recycling of obsolete printed circuit boards
US9221114B2 (en) 2011-12-15 2015-12-29 Advanced Technology Materials, Inc. Apparatus and method for stripping solder metals during the recycling of waste electrical and electronic equipment
US9649712B2 (en) 2011-12-15 2017-05-16 Entegris, Inc. Apparatus and method for stripping solder metals during the recycling of waste electrical and electronic equipment
US9731368B2 (en) 2011-12-15 2017-08-15 Entegris, Inc. Apparatus and method for stripping solder metals during the recycling of waste electrical and electronic equipment

Also Published As

Publication number Publication date
DE1950030A1 (de) 1970-04-30
JPS4816094B1 (enrdf_load_html_response) 1973-05-19
GB1237309A (en) 1971-06-30
FR2020578A1 (enrdf_load_html_response) 1970-07-17
NL6814635A (enrdf_load_html_response) 1970-04-14

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